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Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project

American journal of human genetics, 2020-10, Vol.107 (4), p.596-611

2020

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An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening

The Journal of pediatrics, 2019-06, Vol.209, p.68-76

2019

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Parental Views on Newborn Next Generation Sequencing: Implications for Decision Support

Maternal and child health journal, 2020-07, Vol.24 (7), p.856-864

2020

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Burden or benefit? Effects of providing education about and the option to request additional genomic findings from diagnostic exome sequencing: A randomized controlled trial

Patient education and counseling, 2021-12, Vol.104 (12), p.2989-2998

2021

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Evaluating parents' decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol

Trials, 2018-06, Vol.19 (1), p.344-344, Article 344

2018

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Experiences with obtaining informed consent for genomic sequencing

American journal of medical genetics. Part A, 2015-11, Vol.167A (11), p.2635-2646

2015

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Is “incidental finding” the best term?: a study of patients’ preferences

Genetics in medicine, 2017-02, Vol.19 (2), p.176-181

2017

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"Possibly positive or certainly uncertain?": participants' responses to uncertain diagnostic results from exome sequencing

Genetics in medicine, 2018-03, Vol.20 (3), p.313-319

2018

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Moving toward NextGenetic counseling

Genetics in medicine, 2012-09, Vol.14 (9), p.777-778

Roche, Myra I

2012

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A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

Genetics in medicine, 2016-05, Vol.18 (5), p.467-475

2016

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Supporting Parental Decisions About Genomic Sequencing for Newborn Screening: The NC NEXUS Decision Aid

Pediatrics (Evanston), 2016-01, Vol.137 Suppl 1, p.S16

2016

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The who, what, and why of research participants’ intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study

Genetics in medicine, 2018-07, Vol.20 (7), p.760-769

2018

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It’s time to ramp up genetic counseling training

Genetics in medicine, 2016-08, Vol.18 (8), p.768-769

2016

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Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete-choice experiment

Genetics in medicine, 2018-02, Vol.20 (2), p.181-189

2018

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Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes

Genetics in medicine, 2020-01, Vol.22 (1), p.60-68

2020

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“Not Tied Up Neatly with a Bow”: Professionals’ Challenging Cases in Informed Consent for Genomic Sequencing

Journal of genetic counseling, 2016-02, Vol.25 (1), p.62-72

2016

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Genetic Information, Non-Discrimination, and Privacy Protections in Genetic Counseling Practice

Journal of genetic counseling, 2014-12, Vol.23 (6), p.891-902

2014

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Factors influencing NCGENES research participants' requests for non-medically actionable secondary findings

Genetics in medicine, 2019-05, Vol.21 (5), p.1092-1099

2019

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Correction: Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes

Genetics in medicine, 2019-12, Vol.21 (12), p.2846-2846

2019

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Development and Validation of a Genomic Knowledge Scale to Advance Informed Decision-Making Research in Genomic Sequencing

MDM policy & practice, 2017, Vol.2 (1), p.238146831769258

2017

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How Parents Search, Interpret, and Evaluate Genetic Information Obtained from the Internet

Journal of genetic counseling, 2009-04, Vol.18 (2), p.119-129

2009

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A case of genetic counselling for Dr Watson

Nature (London), 2008-05, Vol.453 (7193), p.281-281

Roche, Myra I

2008

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The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: Report and review

American journal of medical genetics. Part A, 2015-09, Vol.167A (9), p.2176-2181

2015

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How Can Psychological Science Inform Research About Genetic Counseling for Clinical Genomic Sequencing?

Journal of genetic counseling, 2015-04, Vol.24 (2), p.193-204

2015

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Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project

An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening

Parental Views on Newborn Next Generation Sequencing: Implications for Decision Support

Burden or benefit? Effects of providing education about and the option to request additional genomic findings from diagnostic exome sequencing: A randomized controlled trial

Evaluating parents' decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol

Experiences with obtaining informed consent for genomic sequencing

Is “incidental finding” the best term?: a study of patients’ preferences

"Possibly positive or certainly uncertain?": participants' responses to uncertain diagnostic results from exome sequencing

Moving toward NextGenetic counseling

A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

Supporting Parental Decisions About Genomic Sequencing for Newborn Screening: The NC NEXUS Decision Aid

The who, what, and why of research participants’ intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study

It’s time to ramp up genetic counseling training

Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete-choice experiment

Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes

“Not Tied Up Neatly with a Bow”: Professionals’ Challenging Cases in Informed Consent for Genomic Sequencing

Genetic Information, Non-Discrimination, and Privacy Protections in Genetic Counseling Practice

Factors influencing NCGENES research participants' requests for non-medically actionable secondary findings

Correction: Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes

Development and Validation of a Genomic Knowledge Scale to Advance Informed Decision-Making Research in Genomic Sequencing

How Parents Search, Interpret, and Evaluate Genetic Information Obtained from the Internet

Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Sequencing (NCGENES) 2 study: a randomized controlled trial

A case of genetic counselling for Dr Watson

The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: Report and review

How Can Psychological Science Inform Research About Genetic Counseling for Clinical Genomic Sequencing?

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